FDA.reportPublic FDA data

Koobarra Mineral Face Sunscreen SPF 50

Manufacturer
VEGANIC SKN LIMITED
Effective date
2026-01-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:31:59

Label at a glance#

ProductKoobarra Mineral Face Sunscreen SPF 50
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc oxide - 25%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

kindly refer to label picture

WARNINGS SECTION

For external use only.

Do not use on damaged r broken skin.

When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs.

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

kindly refer to artwork

INACTIVE INGREDIENT SECTION

See ingredients on label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label for Medium TintLabel for Medium Tint

Label for TintedLabel for Tinted

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130199284217591GTIN-13: 0199284217591
EAN-13: 0199284217591
GTIN-12: 199284217591
UPC-A: 199284217591
GTIN storage (14 digits): 00199284217591		Koobarra - Tinted AUST L 407959.jpg
QR code linkQR Codeqrau.co/ps6AezKoobarra - Tinted AUST L 407959.jpg, Koobarra - Medium Tint AUST L 407959.jpg
QR code linkQR Codeqrco.de/bgR0ndKoobarra - Tinted AUST L 407959.jpg, Koobarra - Medium Tint AUST L 407959.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83252-104-25Koobarra Mineral Face Sunscreen SPF 500.1 kg in 1 BOTTLE, PUMPCREAM0.12

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83252-10483252-104-25

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM HYALURONATEYSE9PPT4THIACT
SODIUM CHLORIDE451W47IQ8XIACT
GLYCERINPDC6A3C0OXIACT
POLYGLYCERYL-3 RICINOLEATEMZQ63P0N0WIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
CALENDULA OFFICINALIS FLOWERING TOP18E7415PXQIACT
SODIUM ASCORBATES033EH8359IACT
XANTHAN GUMTTV12P4NEEIACT
FERRIC OXIDE RED1K09F3G675IACT
BISABOLOL24WE03BX2TIACT
SODIUM HINOKITIOL5MPS47D679IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
CORIANDER OIL7626GC95E5IACT
ZINC OXIDESOI2LOH54ZACTIB
KAKADU PLUM0ZQ1D2FDLIIACT
CITRUS PARADISI (GRAPEFRUIT) SEED OIL598D944HOLIACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
MALTODEXTRIN7CVR7L4A2DIACT
JOJOBA OIL724GKU717MIACT
HIPPOPHAE RHAMNOIDES SEED OILT53SBG6741IACT
TOCOPHEROLR0ZB2556P8IACT
WATER059QF0KO0RIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
ISOSTEARIC ACIDX33R8U0062IACT
CANDELILLA WAXWL0328HX19IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Koobarra Mineral Face Sunscreen SPF 50ZINC OXIDE SUNSCREENVEGANIC SKN LIMITED37cf8143-99f2-cca5-e063-6394a90a19a82026-01-07WarningsExact identifier
ndc (package): 83252-104-25
ndc (product): 83252-104
ndc11 (package): 83252010425
spl id: 47d6c948-b292-aa4c-e063-6394a90afd32
spl set id: 37cf8143-99f2-cca5-e063-6394a90a19a8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.